C50R (p.Cys50Arg) variant of TNFRSF13B (O14836)
C50R (p.Cys50Arg) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.77 / 1. The record also includes population frequency data.
C50R (p.Cys50Arg) variant details
- p.Cys50Arg
- ExAC rs778514858
- TOPMed rs778514858
- gnomAD rs778514858
- Missense
- Variant Prioritization Score for Impact Estimate 0.767
- REVEL 0.88
- CADD 23.70
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00091)